This is a really hard post for me to write. Usually, I don't write about inside personal struggles; but I feel compelled to talk about it because I think it's a topic that is often ignored or looked over.
For the past few months, I've been struggling with depression and anxiety. I'm self-diagnosing it postpartum depression and anxiety, since I just had a baby.
My world changed. Once sleep-filled Saturdays turned into 2 a.m. necessity baths and 9 p.m. whatever dinners. Even when Cole's sleeping, I'm constantly doing one thing after the other: picking up, making bottles, showering. I have no relax time anymore. It's run, run, run. And it is taking its toll.
More than once I've had to call friends and family in the middle of the night to see if someone - anyone - could come help with Cole. I didn't feel like I could do one more thing. More than once has the sound of him waking over the baby monitor sent anxiety through my veins and made my heart race. I feel guilty even admitting that.
It hit me around the third month. I had gone back to work and Mike was working his week-on/week-off schedule. Life, as it was, returned to "normal." I realized the depression pretty quickly, having had bouts of it on and off in the past. It was the anxiety that I didn't quite recognize. Then one night - Mike was working - I woke up with Cole and couldn't catch my breath. I thought I was going to pass out. Who would take care of my baby if I were to die in the middle of the night with Mike gone?
It was then that I realized that I was having an anxiety attack. I knew I would be OK, but that doesn't get you very far when you can't catch your breath and there's someone in the other room who needs you. At 3:30 a.m. that day, I called my dad, who lives over an hour away, to come keep me company and help out with Cole.
That was the day that I said enough. I needed to cut out a stresser. That day, I decided to quit my job.
Tuesday, July 12, 2011
Monday, July 11, 2011
Quick update
I've been home a little over a month now with Cole and I'm really enjoying it. We stay busy pretty much all day.
When I first quit my job I dreamed of having all this free time...
Yeah, go ahead and laugh.
I do pretty good most days, though. They pass by pretty quickly.
Some days, I wonder how I ever had a job.
When I first quit my job I dreamed of having all this free time...
Yeah, go ahead and laugh.
I do pretty good most days, though. They pass by pretty quickly.
Some days, I wonder how I ever had a job.
Thursday, June 2, 2011
An undone post, but it's all I can do for today
I have a lot of things to talk to you, dear readers, about. But today, I'm going to talk about my mom.
My lovely mother. It is so hard for me to think about this, but I've got to come to terms with it.
My mom has cystic fibrosis. We found this out just a few weeks after my aunt, who also was recently diagnosed with CF, passed away.
I can't imagine how my mom is dealing with this. Seeing your sister die from this awful disease and finding out weeks later that you also have it. I know it's been nerve-wrecking for her. Up 'til now she has had virtually no symptoms of this disease - which in all honesty is probably a really, really good thing.
I haven't been too terribly worried (or maybe I've just been avoiding coming to terms with it) because we're still in the finding-out stages of this. They've done a bazillion tests on her to see what type of CF she has (turns out it's really rare), but they haven't begun treating her fully yet because they're waiting on all the test results first.
It's like I told my friend today - this just came out of nowhere! It makes my head spin to think about it. Most people are diagnosed with this at birth or shortly thereafter, and I don't even want to think about the average lifespan for someone with CF. I am really scared for her.
She is one of the strongest people I know.
My lovely mother. It is so hard for me to think about this, but I've got to come to terms with it.
My mom has cystic fibrosis. We found this out just a few weeks after my aunt, who also was recently diagnosed with CF, passed away.
I can't imagine how my mom is dealing with this. Seeing your sister die from this awful disease and finding out weeks later that you also have it. I know it's been nerve-wrecking for her. Up 'til now she has had virtually no symptoms of this disease - which in all honesty is probably a really, really good thing.
I haven't been too terribly worried (or maybe I've just been avoiding coming to terms with it) because we're still in the finding-out stages of this. They've done a bazillion tests on her to see what type of CF she has (turns out it's really rare), but they haven't begun treating her fully yet because they're waiting on all the test results first.
It's like I told my friend today - this just came out of nowhere! It makes my head spin to think about it. Most people are diagnosed with this at birth or shortly thereafter, and I don't even want to think about the average lifespan for someone with CF. I am really scared for her.
She is one of the strongest people I know.
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